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Neuroinflammatory paradigms in lysosomal storage diseases

Lysosomal storage diseases (LSDs) include approximately 70 distinct disorders that collectively account for 14% of all inherited metabolic diseases. LSDs are caused by mutations in various enzymes/proteins that disrupt lysosomal function, which impairs macromolecule degradation following endosome-ly...

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Detalles Bibliográficos
Autores principales: Bosch, Megan E., Kielian, Tammy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627351/
https://www.ncbi.nlm.nih.gov/pubmed/26578874
http://dx.doi.org/10.3389/fnins.2015.00417

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